Data Coordinator
The START Center for Cancer Research
Summary
The START Center for Cancer Research ("START") is the world's largest early phase site network, fully dedicated to oncology clinical research. We are seeking a Data Coordinator. This role will collect, enter/transcribe, and transmit/submit clinical data for assigned investigational drug studies.
Job description
Essential Responsibilities
- Collect, enter/transcribe, and transmit/submit clinical data in paper and/or electronic case report forms (CRFs), including correction and query resolution for assigned investigational drug studies.
- Receive and request patient records/data from the study team as required to complete CRFs for assigned studies.
- Review patient data for completeness and accuracy for assigned studies.
- Coordinate and schedule monitor visits for assigned studies, including exit meetings with monitors to review data or queries.
- Identify lab facilities used for assigned studies and communicate to the Regulatory Affairs staff so that lab certifications can be requested for the study file.
- Review and utilize protocols as guides for study activities for assigned studies.
- Assure that data entry remains current for all assigned studies.
- Attend meetings as required for assigned studies, including site initiation meetings, monitor exit meetings, close-out visit meetings, and audit preparation meetings.
Required Education and Experience
- High School Diploma/GED.
- 2 years of clinical data entry experience.
- Knowledge and training in general office administration skills, including computer applications, filing systems.
Preferred Education and Experience
- Bachelor's degree.
- Ability to accurately perform data review and CRF completion in its entirety with minimal direction.
- Familiarity with medical terminology.
- CCRP or CCRC credentials.
Physical and Travel Requirements
- Travel required up to 10% of the time.
- Sitting for extended periods of time.
- Typing and computer use for extended periods of time.
Requirements
- High School Diploma/GED
- 2 years of clinical data entry experience
- Knowledge and training in general office administration skills, including computer applications, filing systems
- Bachelor's degree (preferred)
- Ability to accurately perform data review and CRF completion with minimal direction (preferred)
- Familiarity with medical terminology (preferred)
- CCRP or CCRC credentials (preferred)
Benefits
- 401(k) Matching
- Annual Performance Bonus
- Paid Time Off
- Paid Holidays
- Medical, Dental & Vision
- Life & Disability Insurance
- Employee Assistance Program
- Flexible FSA & HSA
Company overview
The START Center for Cancer Research (START) is a global leader in early-phase oncology clinical trials, providing specialized access to novel anti-cancer therapies through its extensive network of community-based research sites. Founded in Texas in 2007, START has established itself as the world's largest community-based early-phase oncology research organization with operations spanning the United States and Europe. The company operates 10 research locations globally and has conducted over 1,500 early-phase clinical trials, contributing to the development and approval of 45 FDA/EMA-approved cancer therapies. START's unique model embeds clinical trial capabilities within community oncology centers, enabling patients to access cutting-edge treatments where they already receive care. With more than 30 Principal Investigators and over 100,000 square feet of world-class research facilities, the organization focuses on accelerating the transition from clinical trials to approved treatments. START's comprehensive approach includes genetic tumor profiling, targeted therapies, and multi-specialty services, all delivered through a patient-centered framework that prioritizes accessibility and scientific rigor in cancer research.